Variant report

Variant	rs369026
Chromosome Location	chr14:78601785-78601786
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs452256	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8022472	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8022610	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs888412	0.83[ASN][1000 genomes]

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78598600-78613000	Weak transcription	Brain Substantia Nigra	brain
2	chr14:78600800-78601800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:78600800-78603000	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr14:78601000-78603400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr14:78601400-78602000	Enhancers	NHEK	skin
6	chr14:78601400-78603000	Enhancers	Primary hematopoietic stem cells	blood
7	chr14:78601400-78603200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr14:78601600-78602600	Flanking Active TSS	A549	lung
9	chr14:78601600-78603000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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